@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_head {
  this: np:hasAssertion dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion;
    np:hasProvenance dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_provenance;
    np:hasPublicationInfo dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion a np:Assertion .
  
  dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_provenance a np:Provenance .
  
  dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0000809 a ncit:C7057 .
  
  dgn-gda:DGN67b06aef26591c3f6bcc0a9654c5ead1 sio:SIO_000628 miriam-gene:2147, lld:C0000809;
    a sio:SIO_001122 .
}

dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_provenance {
  dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion dcterms:description
      "[Our study did not demonstrate that women who are carriers of the factor V, prothrombin, or MTHFR mutations are at higher risk of recurrent fetal loss than women without these mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:12380673;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}